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伊布替尼和利妥昔单抗联合环磷酰胺、多柔比星、长春新碱和泼尼松治疗非生发中心 B 细胞弥漫性大 B 细胞淋巴瘤的随机 III 期临床试验。

Randomized Phase III Trial of Ibrutinib and Rituximab Plus Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone in Non-Germinal Center B-Cell Diffuse Large B-Cell Lymphoma.

机构信息

1 Memorial Sloan Kettering Cancer Center, New York, NY.

2 BC Cancer Agency, Vancouver, British Columbia, Canada.

出版信息

J Clin Oncol. 2019 May 20;37(15):1285-1295. doi: 10.1200/JCO.18.02403. Epub 2019 Mar 22.

Abstract

PURPOSE

Ibrutinib has shown activity in non-germinal center B-cell diffuse large B-cell lymphoma (DLBCL). This double-blind phase III study evaluated ibrutinib and rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) in untreated non-germinal center B-cell DLBCL.

PATIENTS AND METHODS

Patients were randomly assigned at a one-to-one ratio to ibrutinib (560 mg per day orally) plus R-CHOP or placebo plus R-CHOP. The primary end point was event-free survival (EFS) in the intent-to-treat (ITT) population and the activated B-cell (ABC) DLBCL subgroup. Secondary end points included progression-free survival (PFS), overall survival (OS), and safety.

RESULTS

A total of 838 patients were randomly assigned to ibrutinib plus R-CHOP (n = 419) or placebo plus R-CHOP (n = 419). Median age was 62.0 years; 75.9% of evaluable patients had ABC subtype disease, and baseline characteristics were balanced. Ibrutinib plus R-CHOP did not improve EFS in the ITT (hazard ratio [HR], 0.934) or ABC (HR, 0.949) population. A preplanned analysis showed a significant interaction between treatment and age. In patients age younger than 60 years, ibrutinib plus R-CHOP improved EFS (HR, 0.579), PFS (HR, 0.556), and OS (HR, 0.330) and slightly increased serious adverse events (35.7% 28.6%), but the proportion of patients receiving at least six cycles of R-CHOP was similar between treatment arms (92.9% 93.0%). In patients age 60 years or older, ibrutinib plus R-CHOP worsened EFS, PFS, and OS, increased serious adverse events (63.4% 38.2%), and decreased the proportion of patients receiving at least six cycles of R-CHOP (73.7% 88.8%).

CONCLUSION

The study did not meet its primary end point in the ITT or ABC population. However, in patients age younger than 60 years, ibrutinib plus R-CHOP improved EFS, PFS, and OS with manageable safety. In patients age 60 years or older, ibrutinib plus R-CHOP was associated with increased toxicity, leading to compromised R-CHOP administration and worse outcomes. Further investigation is warranted.

摘要

目的

伊布替尼已显示出在非生发中心 B 细胞弥漫性大 B 细胞淋巴瘤(DLBCL)中的活性。这项双盲 III 期研究评估了伊布替尼联合利妥昔单抗和环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)在未经治疗的非生发中心 B 细胞 DLBCL 患者中的疗效。

患者和方法

患者以 1:1 的比例随机分配至伊布替尼(每天口服 560mg)联合 R-CHOP 或安慰剂联合 R-CHOP。主要终点是意向治疗(ITT)人群和激活 B 细胞(ABC)DLBCL 亚组的无事件生存(EFS)。次要终点包括无进展生存(PFS)、总生存(OS)和安全性。

结果

共 838 例患者被随机分配至伊布替尼联合 R-CHOP(n=419)或安慰剂联合 R-CHOP(n=419)。中位年龄为 62.0 岁;75.9%的可评估患者患有 ABC 亚型疾病,且基线特征均衡。伊布替尼联合 R-CHOP 并未改善 ITT(风险比[HR],0.934)或 ABC(HR,0.949)人群的 EFS。一项预先计划的分析显示,治疗与年龄之间存在显著的交互作用。在年龄小于 60 岁的患者中,伊布替尼联合 R-CHOP 改善了 EFS(HR,0.579)、PFS(HR,0.556)和 OS(HR,0.330),并略微增加了严重不良事件(35.7% 28.6%),但治疗组之间接受至少 6 个周期 R-CHOP 的患者比例相似(92.9% 93.0%)。在年龄 60 岁或以上的患者中,伊布替尼联合 R-CHOP 恶化了 EFS、PFS 和 OS,增加了严重不良事件(63.4% 38.2%),并降低了接受至少 6 个周期 R-CHOP 的患者比例(73.7% 88.8%)。

结论

该研究在 ITT 或 ABC 人群中未达到主要终点。然而,在年龄小于 60 岁的患者中,伊布替尼联合 R-CHOP 改善了 EFS、PFS 和 OS,且安全性可控。在年龄 60 岁或以上的患者中,伊布替尼联合 R-CHOP 与毒性增加相关,导致 R-CHOP 给药受损和结局恶化。需要进一步研究。

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